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Human Disease

primary ciliary dyskinesia 25

Term ID
DOID:0110615
Synonyms
  • CILD25
  • primary ciliary dyskinesia 25 with or without situs inversus
Definition
A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with inner and outer dynein arm defect, recurrent upper and lower airway disease, bronchiectasis, decreased fertility and variable occurence of laterality defects and has_material_basis_in homozygous or compound heterozygous mutation in the DYX1C1 gene on chromosome 15q21. (2)
References
Ontology
Human Disease   ( DOID:0110615 )
Relationships
is a type of
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Genes Involved
Zebrafish Models
Citations